Home/Recalls/FDA-Z-2071-2026
FDA DevicesClass II

DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Asymmetrical Tano Forceps, Model/C...

Published: May 13, 2026Recall ID: Z-2071-2026Category: devicesCountry: US

Reason for Recall / Hazard

Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

Product Description & Identification

DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Asymmetrical Tano Forceps, Model/Catalog Number: DVF4014-25-S

Additional Source Details

FieldValue
CityChesterfield
StateMO
Event id98660
Address 1722 Goddard Ave
Code infoLot Code: Model No: DVF4014-25-S UDI-DI: (01)10840096205111(11)250909(17)280909(10)M49277 Lot Number: M49277 Expiration Date: 09/09/2028 Model No: DVF4014-25-S UDI-DI: (01)10840096205111(11)250513(17)280513(10)M47588, Lot Number: M47588 Expiration Date: 05/13/2028 Model No: DVF4014-25-S UDI-DI: (01)10840096205111(11)250506(17)280506(10)M47364, Lot Number: M47364 Expiration Date: 05/06/2028 Model No: DVF4014-25-S UDI-DI: (01)10840096205111(11)250506(17)280506(10)M47363 Lot Number: M47363 Expiration Date: 05/06/2028
Postal code63005-1100
Report date20260513
Product typeDevices
Product quantity80 units
Reason for recallField Safety Corrective Action for IFU in DEX Forceps and Scissors.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260325
Initial firm notificationLetter
Center classification date20260506

Overview

  • Recalling FirmKatalyst Surgical, LLC
  • StatusOngoing
  • Risk LevelClass II
  • DistributionWorldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France.
Official Agency Alert